Canonical Allele Identifier: CA358950441

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130297T>G (hg19) ; chr4:g.186209143T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209143T>G , CM000666.2:g.186209143T>G	GRCh38
NC_000004.11:g.187130297T>G , CM000666.1:g.187130297T>G	GRCh37
NC_000004.10:g.187367291T>G	NCBI36
NG_007965.1:g.22624T>G
NG_012095.2:g.5165T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1276T>G (CYP4V2) MANE Select	ENSP00000368079.4:p.Leu426Val
ENST00000378802.4:c.1276T>G (CYP4V2)	ENSP00000368079.4:p.Leu426Val
ENST00000502665.1:n.511T>G (CYP4V2)
ENST00000507209.5:n.5974T>G (CYP4V2)
ENST00000511608.5:c.72T>G (KLKB1)
ENST00000513354.5:n.366T>G (CYP4V2)
NM_207352.3:c.1276T>G (CYP4V2)	NP_997235.3:p.Leu426Val
XM_005262935.2:c.1273T>G (CYP4V2)	XP_005262992.1:p.Leu425Val
XM_006714184.2:c.880T>G (CYP4V2)	XP_006714247.1:p.Leu294Val
XM_005262935.4:c.1273T>G (CYP4V2)	XP_005262992.1:p.Leu425Val
XM_017008037.1:c.880T>G (CYP4V2)	XP_016863526.1:p.Leu294Val
NM_207352.4:c.1276T>G (CYP4V2) MANE Select	NP_997235.3:p.Leu426Val